REYNOLDS BLEACHING PROCESS— 510(k) K790378

Name: FDA 510(k) clearance K790378
Creator: U.S. Food and Drug Administration
Published: 1979-04-10

Substantially Equivalent

Reynolds Laboratories

FDA 510(k) clearance K790378 for REYNOLDS BLEACHING PROCESS, Substantially Equivalent on 1979-04-10. Applicant: Reynolds Laboratories. Device class: 1.

Clearance details

Applicant: Reynolds Laboratories
Product code: Code EEG
Device class: Class 1
Regulation: 21 CFR 872.6475
Advisory panel: Dental
Date received: 1979-02-23
Decision date: 1979-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EEG

view all

K122725 — TANDA PEARL, ULTRAWYTE, PEARL2012-11-27
K110888 — ABSOLUTE WHITE LIGHT2012-01-12
K063704 — BRITEWHITE TEETH WHITENING SYSTEM, MODEL BW11012007-02-20
K052040 — QUICKSMILE2005-10-18
K041392 — SONX 35 ULTRASONIC BLEACHING SYSTEM; SONIWHITE ULTRA SONIC, MODEL QUICK WHITE US2004-11-08

Data sourced from openFDA. This site is unofficial and independent of the FDA.